CANNULATED METALLIC HEMI TOE IMPLANT, MODELS MPJ241975, MPJ221775, MPJ211675, MPJ191565, MPJ171365


Device Classification Name

prosthesis, toe, hemi-, phalangeal

510(k) Number K023684
Device Name CANNULATED METALLIC HEMI TOE IMPLANT, MODELS MPJ241975, MPJ221775, MPJ211675, MPJ191565, MPJ171365
Original Applicant
VILEX, INC.
345 old curry hollow rd.
pleasant hills, 
PA 
15236

Original Contact abraham lavi
Regulation Number 888.3730
Classification Product Code
KWD  
Date Received 11/01/2002
Decision Date 03/01/2004
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Orthopedic

510k Review Panel

Orthopedic

statement

statement

Type Traditional
Reviewed by Third Party No

Combination Product

No